Pubertede Koroner Revaskülarizasyon ve Ailesel Hiperlipidemi:
Greft Seçimi
FAMILIAL HYPERLIPIDEMIA AND PUBERTAL CORONARY
REVASCULARIZATION: GRAFT SELECTION
Kývanç Metin, *Öztekin Oto, *Baran Uðurlu, *Nejat Sarýosmanoðlu, *Eyüp Hazan, **Adnan Akçoral, **Gül Saylam, **Nurettin Ünal
Ege Saðlýk Hastanesi, Kalp Damar Cerrahisi Bölümü, Ýzmir
*Dokuz Eylül Üniversitesi Týp Fakültesi, Kalp Damar Cerrahisi Ana Bilim Dalý, Ýzmir **Dokuz Eylül Üniversitesi Týp Fakültesi, Pediatrik Kardiyoloji Bilim Dalý, Ýzmir
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Familyal hiperlipidemi, çok erken yaþlarda koroner arter hastalýðýna sebep olabilen malign karakterli nadir bir hastalýktýr. Burada plazma kolesterol düzeyleri kontrol altýna alýnamamýþ 14 yaþýnda bir olguyu sunuyoruz. Büyüme potansiyeli ve açýk kalma oranlarý göz önüne alýndýðýnda greft seçiminin bu olguda önem gösterdiði ortaya çýkmaktadýr. Biz olgumuzda iki adet arteriyel, bir adet de safen ven grefti kullandýk.
Anahtarr kelimelerr: Familyal hiperlipidemi, koroner arter hastalýðý, koroner bypass, greft
Türk Göðüs Kalp Damar Cer Derg 2003;11:188-189
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Familial hyperlipidemia is a rare condition with malignant behavior, resulting in premature coronary artery disease. We report a 14 years old case with undertreated plasma cholesterol levels. Graft selection due to growth potential and patency rates was one of the important problems in this patient. Two arterial grafts and one saphenous vein were implanted for coronary revascularization.
Keyyworrds: Familial hyperlipidemia, coronary artery disease, coronary bypass, graft
Turkish J Thorac Cardiovasc Surg 2003;11:188-189
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Adrres: Dr. Kývanç Metin, Ege Saðlýk Hastanesi, Kalp Damar Cerrahisi Bölümü, Ýzmir e-mmail: kmetin@yahoo.com
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Homozygous familial hypercholesterolemia (FH) is a rare condition with an incidence of 1/1 million births. Excessive levels of plasma cholesterol (> 600 mg/dL) and cutaneous xanthomata are characteristic before the age of 5 years [1]. We operated a 14 years old girl with FH. Although this one is not a unique case, we report it to call attention of the community to graft selection in pediatric cases.
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A 14 years old girl was operated due to osteal occlusions of left main trunk and right coronary artery. In her history, she was hospitalized for evaluation of tumor-like cutaneous plaques over distal joints and diagnosed as xanthoma 9 years ago. Cutaneous symptoms began over her coxycs and spread out to extremities (Figure 1). She had high plasma lipid levels (cholesterol 772 mg/dL; triglycerides 74 mg/dL; HDL 14 mg/dl; LDL 571 mg/dL) and abnormal lipid electrophoresis (a 4.5%, pre-b 9.9%, b 85.4%). Other biochemical parameters were normal. She was weighing 16 kg (3-10 percentile) and 103 cm high (3-10 percentile). The diagnosis was “familial hyperlipidemia type 2a”. Plasma lipid content of her brothers and father were within normal limits. Her mother’s lipid profile was unknown, because she had died accidentally 3 years ago. A dietary program excluding saturated fatty acids and medical treatment was
planned. No neurological, cardiac or ophthalmic pathology was noted. After medical treatment and dietary suggestions, the result was desperate after 5 months: cholesterol 614 mg/dL and triglyceride 123 mg/dL. Probably, she was not obeying to the regimen. Closer follow-up with monthly intervals was planned. Because the family was living in a rural area, it was not easy to perform frequent visits. Cholesterol levels ranged between 444 to 817 mg/dL despite all medical attempts. Plasmapheresis was not performed due to discordance of her family. She came to control for the last time on July 1992. She reappeared with stable angina pectoris on August 1998. Physical examination was almost normal. Cutaneous lesions were persevering and a slight systolic murmur over pulmonary valve was heard. Morphological findings on echocardiography were normal, with 70% ejection fraction and 39% fractional shortening. Cholesterol level was 583 mg/dL (LDL 535 mg/dL, HDL 35 mg/dL) and triglyceride 64 mg/dL. A treadmill test was planned and pravastatine 10 mg/day was added to regimen. After another long period of disappearance, treadmill test was performed on May 2000, with a non-surprising positive result. Coronary angiography showed a 40% narrowing of left main trunk, and cholesterol levels were very high (total 629 mg/dL, HDL 46 mg/dL, LDL 569 mg/dL, triglyceride 70 mg/dL). Pravastatin was doubled (20 mg/day), aspirin 300 mg/day and metoprolol was added. There were no cardiac symptoms until November 2001. Then she was hospitalized with severe unstable angina pectoris. Angiographic examination showed 70% occlusions of
Metin et al
Familial Hyperlipidemia Graft Selection
both left main trunk and right coronary artery, and a normal ventriculography. An urgent coronary artery bypass grafting was mandatory for this child. Graft selection was right internal mammarian artery (IMA) for the right coronary artery, left IMA for the left anterior descending artery and greater saphenous vein graft for the circumflex artery. She weaned from cardiopulmonary bypass with the aid of intra-aortic balloon counterpulsation (IABP), which was removed 4 hours postoperatively. Inotropic support was ceased on the first postoperative day.
This patient is now under strict follow-up and two sessions of plasmapheresis have been performed. Plasma cholesterol levels lowered significantly (total cholesterol 291 mg/dL; LDL 231 mg/dL; HDL 37 mg/dL) and the result of a control treadmill test 3 months after the operation was negative.
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As coronary artery disease (CAD) is the major cause of death in western world, dyslipidemia is one of the most important risk factors of it [2]. Particularly younger patients with dyslipidemia may have rapidly occlusive disease. Most of these cases are resistant to anti-hypercholesterolemic treatment. The proportion of plasma cholesterol contents influences the behavior of the disease and strongly correlated with clinical outcome of patients. There patients developing CAD have significantly lower values of plasma high density lipoprotein cholesterol levels and a higher ratio of total cholesterol/HDL when compared with patients free of CAD [3]. Usually, medical treatment doesn’t give any satisfying results. Familial hyperlipidemia may have a morbid nature. Significant narrowing of the coronary arteries may result in premature cardiac death during childhood. Clinical condition is very similar to that of middle age individuals’ atherosclerotic coronary artery disease. But pathological
examinations have showed that the vascular lesion is not an atheromatous plaque, but a xanthomatous deposit of excessive plasma cholesterol [4]. Coronary revascularization improves the long term survival in those patients. From the surgical point of view, selection of grafts is the main question. Arterial revascularization offers better late-cardiac-event-free survival. But according to the literary data, we have avoided from extensive use of arterial conduits (radial or right gastroepiploic arteries), which does not have additional benefit or cost [5]. We have anastomosed the right internal thoracic artery to the right coronary artery, and the left internal thoracic artery to the left anterior descending coronary artery. Blood supply to circumflex system was maintained with a greater saphenous vein graft. A relatively longer saphenous vein was anastomosed to circumflex artery to overcome the potential shrinkage of the graft with growing up of the child. Complete occlusion of venous grafts is almost a rule in patients under 5 years of age, but patency rate improves in those over 10 years. Rapid degeneration of the vein and increasing body size of the patient may be reasons of graft failure [7]. On the other side, arterial grafts have the growth potential. We have explained early postoperative period of low cardiac out-put by chronic ischemia of the young myocardium. The stunning heart responded very well after 4 hours of IABP support.
This case was the first pediatric coronary bypass surgery due to familial hyperlipidemia in our institution. Good information of the family members and peer follow-up will be mandatory for this patient.
“Prof. Dr. Adnan Akçoral (1945-2003) anýsýna”
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1. Demetriou K, H’Maltezou E, Pierides AM. Familial homozygous hypercholesterolemia: Effective long-term treatment with cascade double filtration plasmapheresis. Blood Purif 2001;19:308-13.
2. Voors-Pette C, de Bruin TW. Excess coronary heart disease in Familial Combined Hyperlipidemia, in relation to genetic factors and central obesity. Atherosclerosis 2001;157:481-9.
3. Real JT, Chaves FJ, Martinez-Uso I, Garcia-Garcia AB, Ascaso JF, Carmena R. Importance of HDL cholesterol levels and the total/HDL cholesterol ratio as a risk factor for coronary heart disease in molecularly defined heterozygous familial hypercholesterolemia. Eur Heart J 2001;22:465-71.
4. Stehbens WE. Coronary heart disease, hypercholesterolemia, and atherosclerosis. I. False premises. Exp Mol Pathol 2001;70:103-19.
5. Kawasuji M, Sakakibara N, Fujii S, Yasuda T, Watanabe Y. Coronary artery bypass surgery with arterial grafts in familial hypercholesterolemia. J Thorac Cardiovasc Surg 2000;119:1008-13.
6. Kawasuji M, Sakakibara N, Takemura H, Matsumoto Y, Mabuchi H, Watanabe Y. Coronary artery bypass grafting in familial hypercholesterolemia. J Thorac Cardiovasc Surg 1995;109:364-9.
7. Yoshikawa Y, Yagihara T, Kameda Y, et al. Result of surgical treatments in patients with coronary-arterial obstructive disease after Kawasaki disease. Eur J Cardio-thorac Surg 2000;17:515-9.
189 Figure 1 A and B. Cutaneous xanthomata on the extremities.
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Metin ve Arkadaþlarý Ailesel Hiperlipidemide Greft Seçimi Türk Göðüs Kalp Damar Cer Derg
